The Synergistic Effect of Photoelectrochemical (PEC) Reactions Exemplified by Concurrent Perfluorooctanoic acid (PFOA) Degradation and Hydrogen Generation over Carbon and Nitrogen codoped TiO2 Nanotube Arrays (C-N-TNTAs) photoelectrode

被引:72
作者
Peng, Yen-Ping [1 ]
Chen, Hanlin [1 ]
Huang, C. P. [2 ]
机构
[1] Tunghai Univ, Dept Environm Sci & Engn, Taichung 40704, Taiwan
[2] Univ Delaware, Dept Civil & Environm Engn, Newark, DE 19716 USA
关键词
Photoelectrochemical; C-N-TNTA; PFOA; Hydrogen; Synergetic effect; VISIBLE-LIGHT PHOTOCATALYSIS; SPIN-TRAPPING DETECTION; SENSITIZED SOLAR-CELLS; PERFLUOROCARBOXYLIC ACIDS; HIGHLY EFFICIENT; ELECTROCHEMICAL MINERALIZATION; ELECTRONIC-PROPERTIES; TITANIUM-OXIDES; FILM ELECTRODE; DECOMPOSITION;
D O I
10.1016/j.apcatb.2017.02.084
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We studied the synergistic effect of photoelectrochemical reactions exemplified by concurrent oxidization of perfluorooctanoic acid (PFOA) and hydrogen generation over carbon and nitrogen codoped TiO2 nanotube arrays (C-N-TNTAs) photoanode. The synthesized C-N-TNTAs were characterized by extended X-ray absorption fine structure (EXAFS) and X-ray diffraction (XRD) and results confirmed the successful doping of carbon and nitrogen into the TNTAs framework without altering its crystalline structure. Mott-Schottky analysis yielded a donor density of 3.547 x 10(18)/cm(3) and 1.159 x 10(18)/cm(3) for TNTA and C-N-TNTA, respectively. The photogenerated electrons had a lifetime (tau(el)) of 2.52, 4.01, and 6.34 ms under biased potential of 0, 0.5, and 1.0V (vs. Ag/AgC1), respectively, indicating the increase in lifetime of phtogenerated electrons in photoelectrochemical (PEC) process. The synergetic effect was further quantified in terms of current/time profile at bias potential of 0 V at 1.1 mA and 1 V at 3.1 mA, individually. Results showed an increase in synergetic efficiency of 56 and 65% at a biased potential of 0.5 and 1.0 V, respectively. PEC effectively separated the photogenerated electron-hole pairs and enhanced the oxidation and reduction capability of the system. PFOA removal reached 56.1% in 180 min (initial concentration =40 mg/L) over the C-N-TNTA photoanode in PEC mode. Results showed that perfluorooctanate, C7F15COO-, was first adsorbed on the C-N-TNTA anode surface followed by formation of C6F13COO(-) after losing CF2 units. Results of electron spin resonance (ESR) further confirmed that reactive species such as (OH)-O-center dot and CH3 center dot were responsible for the decomposition of PFOA during PEC reactions. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:437 / 446
页数:10
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